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草鱼C5a、C5aR和FⅡ多克隆抗体的制备与表达特性
引用本文:苏杭,肖调义,许宝红,刘巧林,吕丽刚,刘益.草鱼C5a、C5aR和FⅡ多克隆抗体的制备与表达特性[J].水产学报,2022,46(5):785-796.
作者姓名:苏杭  肖调义  许宝红  刘巧林  吕丽刚  刘益
作者单位:湖南农业大学,湖南农业大学,湖南农业大学,湖南农业大学,湖南农业大学,湖南农业大学
基金项目:国家自然科学基金联合基金重点支持项目 (U20A2063);湖南省自然科学基金青年项目(2019JJ50265)
摘    要:为研究草鱼补体蛋白5a (complement component 5a,C5a)、补体蛋白5a受体(C5a receptor,C5aR)和凝血因子Ⅱ(blood coagulation factorⅡ,FⅡ)在感染草鱼呼肠孤病毒(grass carp reovirus,GCRV)时的蛋白表达和相互作用,针对草鱼C5a和FⅡ蛋白构建了原核表达体系、针对草鱼C5aR蛋白构建C5aR-KLH偶联物,纯化蛋白,免疫日本大耳白兔制备3种蛋白的多克隆抗体。用蛋白质印迹(Western blot)、免疫共沉淀(Co-IP)和拉下(pull down)实验检测3种蛋白表达与互作关系,Western blot结果显示,C5a和C5aR在健康草鱼的肝脏、脾脏、肾脏、头肾、肠、鳃和肌肉中均有蛋白表达,FⅡ在肝脏、脾脏和肠中表达,而在肾脏、头肾、鳃和肌肉中不表达;在感染GCRV的草鱼肝脏组织中C5a、C5aR和FⅡ蛋白均随病程进展呈现上升趋势。Co-IP结果显示,在GCRV处理后,C5a、C5aR和FⅡ蛋白具有相互作用关系。pull down结果显示,C5a pull down共鉴定得到C3、RIG-I等2...

关 键 词:草鱼  C5a  C5aR  FⅡ  多克隆抗体  草鱼呼肠孤病毒(GCRV)  表达特性
收稿时间:2021/11/19 0:00:00
修稿时间:2022/2/6 0:00:00

Preparation and expression characteristics of polyclonal antibodies against C5a, C5aR and FII in grass carp (Ctenopharyngodon idellus)
SU Hang,XIAO Tiaoyi,XU Baohong,LIU Qiaolin,LV Ligang and LIU Yi.Preparation and expression characteristics of polyclonal antibodies against C5a, C5aR and FII in grass carp (Ctenopharyngodon idellus)[J].Journal of Fisheries of China,2022,46(5):785-796.
Authors:SU Hang  XIAO Tiaoyi  XU Baohong  LIU Qiaolin  LV Ligang and LIU Yi
Institution:Hunan Engineering Technology Research Center of Featured Aquatic Resources Utilization,Hunan Agricultural University,Hunan Engineering Technology Research Center of Featured Aquatic Resources Utilization,Hunan Agricultural University,Hunan Engineering Technology Research Center of Featured Aquatic Resources Utilization,Hunan Agricultural University,Hunan Engineering Technology Research Center of Featured Aquatic Resources Utilization,Hunan Agricultural University,Hunan Engineering Technology Research Center of Featured Aquatic Resources Utilization,Hunan Agricultural University,Hunan Engineering Technology Research Center of Featured Aquatic Resources Utilization,Hunan Agricultural University
Abstract:Complement and coagulation cascade are important components of innate immunity, in which complement protein 5a (complement component 5a, C5a), complement protein 5a receptor (C5a receptor, C5aR) and coagulation factor II (blood coagulation factor II, FII) play a key role in dealing with virus infection. In order to study the protein expression and interaction of Ctenopharyngodon idellus (C. idellus) infected with grass carp reovirus (GCRV), the prokaryotic expression system of C5a and FII protein was constructed, the C5aR-KLH conjugate against C5aR protein was constructed, and the protein was purified. Japanese big-eared rabbits were immunized to prepare polyclonal antibodies against three kinds of proteins. The expression and interaction of the three proteins were detected by western blot, Co-immunoprecipitation (Co-IP) and pulldown test. Western blot results showed that C5a and C5aR proteins were expressed in liver, spleen, kidney, head kidney, intestine, gill and muscle of C. idellus. FII protein was expressed in liver, spleen and intestine, but not in kidney, head kidney, gill and muscle. C5a, C5aR and FII proteins in liver tissues of C. idellus infected with GCRV showed an upward trend with the progression of the disease. Co-IP results showed that C5a, C5aR and FII proteins interacted with each other after GCRV treatment. Pull down results showed that 28 candidate proteins such as C3 and RIG-I were identified by C5a pull down, and 24 candidate proteins such as transaldolase and macroglobulin were identified by C5aR pull down. This study provides a basis for further exploring the interaction and regulation of C5a, C5aR and FII, and for further exploring the mechanism of the three associated proteins in the complement and coagulation cascade system responding to GCRV infection.
Keywords:Ctenopharyngodon idellus  C5a  C5aR  FII  polyclonal antibody  GCRV  expression characteristics
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